Veterinary Medicines

Footvax Emulsion for Injection for Sheep

Authorised
  • Dichelobacter nodosus, serotype H, Inactivated
  • Dichelobacter nodosus, serotype G, Inactivated
  • Dichelobacter nodosus, serotype F, Inactivated
  • Dichelobacter nodosus, serotype E, Inactivated
  • Dichelobacter nodosus, serotype D, Inactivated
  • Dichelobacter nodosus, serotype C, Inactivated
  • Dichelobacter nodosus, serotype B2, Inactivated
  • Dichelobacter nodosus, serotype B1, Inactivated
  • Dichelobacter nodosus, serotype A, Inactivated
  • Dichelobacter nodosus, serotype I, Inactivated
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Product identification

Medicine name:
Footvax Emulsion for Injection for Sheep
Active substance:
  • Dichelobacter nodosus, serotype H, Inactivated
  • Dichelobacter nodosus, serotype G, Inactivated
  • Dichelobacter nodosus, serotype F, Inactivated
  • Dichelobacter nodosus, serotype E, Inactivated
  • Dichelobacter nodosus, serotype D, Inactivated
  • Dichelobacter nodosus, serotype C, Inactivated
  • Dichelobacter nodosus, serotype B2, Inactivated
  • Dichelobacter nodosus, serotype B1, Inactivated
  • Dichelobacter nodosus, serotype A, Inactivated
  • Dichelobacter nodosus, serotype I, Inactivated
Target species:
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Dichelobacter nodosus, serotype H, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype G, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype F, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype E, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype D, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype C, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype B2, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype B1, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype A, Inactivated
    10.00
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dichelobacter nodosus, serotype I, Inactivated
    400.00
    unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Sheep
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI04AB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Cardboard box containing flexible polyethylene vial of 50 ml with rubber stopper and aluminium cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/232/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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